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CCDC40

Gene

coiled-coil domain 40 molecular ruler complex subunit

HGNCHGNC:26090EnsemblENSG00000141519NCBI Gene55036
Locus: gene with protein productLocation: 17q25.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asKIAA1640 · FLJ20753 · FLJ32021 · CILD15 · FAP172 · CFAP172
View full nomenclature history (7)
Alias symbolsKIAA1640, FLJ20753, FLJ32021, CILD15, FAP172, CFAP172
Previous namescoiled-coil domain containing 40

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Kartagener Syndrome
Bronchiectasis
Dry Eye Syndromes

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Cilia and flagella associatedMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-06-12.
Open TargetsGene–disease associations from the Open Targets Platform.